催化作用
化学
高碘酸盐
电子转移
共价键
热解
兴奋剂
无机化学
核化学
化学工程
光化学
降级(电信)
有机化学
材料科学
工程类
电信
光电子学
计算机科学
作者
Lei He,Chao Yang,Jie Ding,Mei-Yun Lu,Cheng-Xin Chen,Guangyuan Wang,Junqiu Jiang,Lan Ding,Guoshuai Liu,Nanqi Ren,Shan-Shan Yang
标识
DOI:10.1016/j.apcatb.2021.120880
摘要
In this study, the performance of periodate (PI) on sulfadiazine (SDZ) degradation was evaluated using coagulation solid waste fabricated catalyst (CWBC), obtained by simple pyrolysis. SDZ effectively underwent 98.94% remove within 90 min in the CWBC/PI system. Electron transfer was the predominant mechanism due to the development of an electronic cycle among SDZ, CWBC and PI, where the O2•−, PFRs, and the reactive iodine species had minor roles. Density functional theory calculations identified that Fe and N could change the electron configuration and break the chemical inertness of carbonaceous material. As a result, electrons on the carbon matrix of CWBC are inclined to travel through the formed Fe–O covalent bond to PI. Further analysis demonstrated that SO42−, humic acid (HA), as well as anoxic conditions greatly facilitated SDZ degradation. This study provides a facile protocol for converting coagulation waste to an efficient catalyst and provides fundamental insights into the degradation mechanisms of micropollutants by activating PI.
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